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MODIFICATION TO: BIOKNOTLESS BR ANCHOR / LUPINE BR ANCHOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070925
510(k) Type
Special
Applicant
Depuy Mitek, A Johnson & Johnson Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2007
Days to Decision
29 days
Submission Type
Summary

MODIFICATION TO: BIOKNOTLESS BR ANCHOR / LUPINE BR ANCHOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070925
510(k) Type
Special
Applicant
Depuy Mitek, A Johnson & Johnson Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2007
Days to Decision
29 days
Submission Type
Summary